Canonical Allele Identifier: PA658832411
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 560190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser82Pro
CA415177504
NM_001110792.2:c.244T>C